Canonical Allele Identifier: CA1468148381
Gene: ALB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73404279C= , CM000666.2:g.73404279C= GRCh38
NC_000004.11:g.74269996C= , CM000666.1:g.74269996C= GRCh37
NC_000004.10:g.74488860C= NCBI36
NG_009291.1:g.5025C=

Transcript Alleles

HGVS Amino-acid change
ENST00000295897.8:c.-49C= ENSP00000295897.4:n.-49C=
ENST00000441319.5:c.48-90C= ENSP00000392541.1:n.48-90C=
ENST00000621628.4:c.-49C= ENSP00000480485.1:n.-49C=
NM_000477.5:c.-49C= NP_000468.1:n.-49C=
NM_000477.6:c.-49C= NP_000468.1:n.-49C=